Basic applied concepts of blood banking and transfusion practices 5th edition

Test Bank For Basic & Applied Concepts of Blood Banking and
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Practices 5th Edition – By Paula Howard
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| Verified Chapter's 1 - 16 | Complete
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,Table of Contents m m




Part I: Quality and Safety Issues
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1. Quality Assurance and Regulation of the Blood Industry: Safety Issues in the Blood Bank…………
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Foundations: Basic Sciences and Reagents
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2. Immunology: Basic Principles and Applications in the Blood Bank ……………………………………………………
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3. Blood Banking Reagents: Overview and Applications……………………………………………………………………1
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in Blood Banking……………………………………………………………………………………….18 Part III: Overview of t
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5. ABO and H Blood Group Systems and Secretor Status…………………………………………………………………
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System……………………………………………………………………………………………………26
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7. Other Red Cell Blood Group Systems, Human Leukocyte Antigens, and Platelet Antigens……………………
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Essentials of Pretransfusion Testing
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8. Antibody Detection and Identification……………………………………………………………………………………34
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m Testing………………………………………………………………………………………………………38

10. Blood Bank Automation for Transfusion Services……………………………………………………………………
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Considerations in Immunohematology
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11. AdverseComplicationsofTransfusions………………………………………………………………………………….46
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12. Hemolytic Disease of the Fetus and Newborn………………………………………………………………………
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Collecting and Testing
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13. Donor Selection and Phlebotomy………………………………………………………………………………………….55
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Blood…………………………………………………………………………………………………….60
m m Part VII: Blood Comp
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Transfusion Therapy
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15. BloodComponentPreparationandTherapy…………………………………………………………………………….63
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16. TransfusionTherapyinSelectedPatients……………………………………………………………………………….. 66
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,Chapter 01: Quality Assurance and Regulation of the Blood Industry and Safety Issues in the Blood Ban
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Applied Concepts of Blood Banking and Transfusion Practices, 5th Edition
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MULTIPLE CHOICE m




1. Biosafety levels determine: m m




a. on what floor certain infectious disease testing can be performed.
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b. the degree of risk for certain areas of a health care facility to exposure to
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minfectious diseases. m




c. the amount of ventilation required in a transfusion service.
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d. how many biohazardous waste containers a laboratory must have.
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ANS: B m




OSHA defines biosafety levels based on potential exposure to infectious material.
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DIF: Level 1 m




2. A laboratory technologist decided she would like to bring her lab coat home for laundering because it ha
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it was returned by the laboratory’s laundry service. Is this practice acceptable?
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a. Yes, if she uses 10% bleach m m m m m




b. Yes, if she clears it with her supervisor
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c. Yes, as long as she removes the coat and does not wear it home
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d. No, because the laboratory is a biosafety level 2, and lab coats may not be
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removed m




ANS: D m




Methods of transporting the lab coat and the risk of contamination do not permit health care workers to
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mcleaning.

DIF: Level 2 m




3. Personal protective equipment includes: m m m




a. safety glasses. m




b. splash barriers. m




c. masks.
d. All of the above m m m




ANS: D m




Safety glasses, splash barriers, and masks are types of personal protective devices.
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DIF: Level 1 m




4. At what point in the employment process should safety training take place?
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a. During orientation and training m m m




b. Following lab training when employees are more familiar with their m m m m m m m m m




mresponsibilities
c. Following the employees’ first evaluation m m m m




d. Before independent work is permitted and annually thereafter
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ANS: D m




The Occupation Safety and Health Administration requires safety training before independent work is pe
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mthereafter.

DIF: Level 1 m

, 7. Which of the following is true regarding good manufacturing practices (GMPs)?
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a. GMPs are legal requirements established by the Food and Drug Administration.
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b. GMPs are optional guidelines written by the AABB. m m m m m m m




c. GMPs are required only by pharmaceutical companies. m m m m m m




d. GMPs are part of the quality control requirements for blood products.
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ANS: A m




Good manufacturing practices are requirements established by the Food and Drug Administration.
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DIF: Level 1 m




8. Which of the following is an example of an unacceptable record-keeping procedure?
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a. Using dittos in columns to save time m m m m m m




b. Recording the date and initials next to a correction m m m m m m m m




c. Not deleting the original entry when making a correction
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d. Always using permanent ink on all records m m m m m m




ANS: A m




All records must be clearly written. Dittos are unacceptable.
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DIF: Level 1 m




9. A technologist in training noticed that the person training her had not recorded the results of a test. To b
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m recorded the results she saw at a later time, using the technologist’s initials. Is this an acceptable proce
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a. Yes; all results must be recorded regardless of who did the test.
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b. No; she should have brought the error to the technologist’s attention.
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c. Yes; because she used the other technologist’s initials.
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d. Yes; as long as she records the result in pencil.
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ANS: B m




This is an example of poor record keeping; results must be recorded when the test is performed and by t
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DIF: Level 3 m




10. Unacceptable quality control results for the antiglobulin test performed in test tubes may be noticed if:
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a. preventive maintenance has not been performed on the cell washer. m m m m m m m m m




b. the technologist performing the test was never trained.
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c. the reagents used were improperly stored.
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d. All of the above m m m




ANS: D m




Training, equipment maintenance, and reagent quality can affect quality control.
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DIF: Level 2 m




11. All of the following are true regarding competency testing except:
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a. it must be performed following training.
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b. it must be performed on an annual basis.
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c. it is required only if the technologist has no experience.
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d. retraining is required if there is a failure in competency testing. m m m m m m m m m m




ANS: C m




All employees must have competency testing following training and annually thereafter. If there is a failu
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mretraining is required. m m




DIF: Level 2 m




12. Which of the following organizations are involved in the regulation of blood banks?
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